You Searched For: 2,2-Difluoroethylamine


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Supplier: TCI America
Description: CAS Number: 370-22-9
MDL Number: MFCD00017925
Molecular Formula: C13H10F2N2O
Molecular Weight: 248.23
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 267

SDS

Catalog Number: (76098-860)
Supplier: Bioss
Description: C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.


Catalog Number: (10666-570)
Supplier: Bioss
Description: C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.


Catalog Number: (89280-496)
Supplier: Genetex
Description: Mouse monoclonal antibody [LOX19-22] to LOX-1 (soluble)


Catalog Number: (TCH0181-005G)
Supplier: TCI America
Description: CAS Number: 16289-95-5
MDL Number: MFCD00003781
Molecular Formula: C18H10O6
Molecular Weight: 322.27
Purity/Analysis Method: >98.0% (T)
Form: Crystal

Supplier: TCI America
Description: CAS Number: 94089-22-2
MDL Number: MFCD00059772
Molecular Formula: C8H12N2O
Molecular Weight: 152.20
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Specific Gravity (20/20): 1.00

SDS

Catalog Number: (TCI0003-005G)
Supplier: TCI America
Description: CAS Number: 570-22-9
MDL Number: MFCD00005200
Molecular Formula: C5H4N2O4
Molecular Weight: 156.10
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 283

SDS


Catalog Number: (10476-324)
Supplier: Bioss
Description: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.


Catalog Number: (TCP1142-025ML)
Supplier: TCI America
Description: CAS Number: 25564-22-1
MDL Number: MFCD00036631
Molecular Formula: C10H16O
Molecular Weight: 152.24
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Color: Colorless
Boiling point (°C): 115
Flash Point (°C): 110
Specific Gravity (20/20): 0.92

SDS


Catalog Number: (10664-264)
Supplier: Bioss
Description: Neuronal axonal membrane protein Nap-22, also designated neuronal tissue-enriched acidic protein or brain acid soluble protein (BASP1), is a Ca2+-dependent calmodulin-binding protein that is important for neuronal sprouting and plasticity. Nap-22 is abundant in brain nerve terminals and is also present in significant amounts in kidney, testis and lymphoid tissue. Nap-22 undergoes N-terminal myristoylation for membrane localization. It has been characterized as a major protein of neuronal rafts, which are known to preferentially bind membranes containing cholesterol. Nap-22 is a crucial protein active in neurite outgrowth and synaptic plasticity.


Supplier: Abcam
Description: Rabbit monoclonal [EPR24997-22] to Calcineurin A.

New Product

Catalog Number: (103889-758)
Supplier: ACROBIOSYSTEMS INC MS
Description: Human IL-22 Protein, His, Avitag*, Biotinylated, Source: expressed from human 293 cells (HEK293). It contains AA Ala 34 - Ile 179, Predicted N-terminus: His, protein carries a polyhistidine tag at the N-terminus, followed by an Avi tag, Synonyms: IL-22, IL-TIF, ZCYTO18, Size: 200uG


Catalog Number: (TCD1498-100MG)
Supplier: TCI America
Description: CAS Number: 1100-22-7
MDL Number: MFCD00069532
Molecular Formula: C18H24N2O4S
Molecular Weight: 364.46
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 126
Specific rotation [a]20/D: -9.5 deg (C=1, EtOH)

Catalog Number: (76121-130)
Supplier: Bioss
Description: C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.


Supplier: TCI America
Description: CAS Number: 6186-22-7
MDL Number: MFCD00210401
Molecular Formula: C9H9BrO
Molecular Weight: 213.07
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 139
Specific Gravity (20/20): 1.42

SDS

Catalog Number: (77516-218)
Supplier: AFG Bioscience
Description: Human IL22Ra2 (Interleukin 22 Receptor Alpha 2) ELISA Kit


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